List of variants in gene NPHP4 reported as uncertain significance by Sydney Genome Diagnostics, Children's Hospital Westmead

Minimum submission review status:		Collection method:
Minimum conflict level: Report conflict between different conditions
Gene type: Distinguish antisense genes from sense genes
Show significances as they were submitted (without aggregation into standard terms)
		ClinVar version:

Total variants: 3

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HGVS	dbSNP	gnomAD frequency
NM_015102.5(NPHP4):c.3329C>T (p.Ala1110Val)	rs139767853	0.00362
NM_015102.5(NPHP4):c.2965G>A (p.Glu989Lys)	rs116606479	0.00062
NM_015102.5(NPHP4):c.871_889delinsC (p.Val291_Phe297delinsLeu)	rs1553186265

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